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New perspectives on molecular targeted therapy in ovarian clear cell carcinoma
Ovarian clear cell carcinomas (OCCCs) account for about 5–13% of all epithelial ovarian carcinomas in Western populations. It is characterised by resistance to conventional platinum-based chemotherapy, and new therapeutic strategies are urgently required. This article will focus on how recent discov...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668466/ https://www.ncbi.nlm.nih.gov/pubmed/23558892 http://dx.doi.org/10.1038/bjc.2013.126 |
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author | Tan, D S P Miller, R E Kaye, S B |
author_facet | Tan, D S P Miller, R E Kaye, S B |
author_sort | Tan, D S P |
collection | PubMed |
description | Ovarian clear cell carcinomas (OCCCs) account for about 5–13% of all epithelial ovarian carcinomas in Western populations. It is characterised by resistance to conventional platinum-based chemotherapy, and new therapeutic strategies are urgently required. This article will focus on how recent discoveries have enhanced our understanding of the molecular pathogenesis of OCCCs, leading to new therapeutic opportunities. These include mutations in ARID1A, which provides a link to endometriosis, upregulation of the phosphatidylinositol 3-kinase/AKT pathway, particularly through mutations of PIK3CA and inactivation of PTEN, and increased activity of pathways involved in angiogenesis. Targeting HER2, apoptotic escape mechanisms and mismatch repair defects offer additional opportunities for treating this enigmatic tumour subtype. |
format | Online Article Text |
id | pubmed-3668466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36684662013-05-31 New perspectives on molecular targeted therapy in ovarian clear cell carcinoma Tan, D S P Miller, R E Kaye, S B Br J Cancer Minireview Ovarian clear cell carcinomas (OCCCs) account for about 5–13% of all epithelial ovarian carcinomas in Western populations. It is characterised by resistance to conventional platinum-based chemotherapy, and new therapeutic strategies are urgently required. This article will focus on how recent discoveries have enhanced our understanding of the molecular pathogenesis of OCCCs, leading to new therapeutic opportunities. These include mutations in ARID1A, which provides a link to endometriosis, upregulation of the phosphatidylinositol 3-kinase/AKT pathway, particularly through mutations of PIK3CA and inactivation of PTEN, and increased activity of pathways involved in angiogenesis. Targeting HER2, apoptotic escape mechanisms and mismatch repair defects offer additional opportunities for treating this enigmatic tumour subtype. Nature Publishing Group 2013-04-30 2013-04-04 /pmc/articles/PMC3668466/ /pubmed/23558892 http://dx.doi.org/10.1038/bjc.2013.126 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Minireview Tan, D S P Miller, R E Kaye, S B New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title | New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title_full | New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title_fullStr | New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title_full_unstemmed | New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title_short | New perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
title_sort | new perspectives on molecular targeted therapy in ovarian clear cell carcinoma |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668466/ https://www.ncbi.nlm.nih.gov/pubmed/23558892 http://dx.doi.org/10.1038/bjc.2013.126 |
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